Remote, Clinical Intelligence Manager

  • Job Reference: 871162456-2
  • Date Posted: 12 January 2023
  • Recruiter: GForce Life Sciences
  • Location: Los Angeles, California
  • Salary: On Application

Job Description


Our mid-sized, growing pharmaceutical client is seeking a Clinical Intelligence Manager consultant. This role will report to the Director of Corporate Projects. The consultant will collaborate across functional areas and ESPs to identify the operational risks, data trends, and data quality for assigned trials or programs.

General Duties / Expectations of Role:

  • Perform regular reviews within the eSurveillance (or alike) system to ensure data quality and performance throughout the life cycle of the study and/or program.
  • Provides frequent input to GCI Leadership and/or Clinical Management Teams on newly identified trends and/or reporting.
  • Provides Project Team and Cross-functional area support to streamline and enhance current data review processes associated with clinical operations and development.
  • Create, maintain, and manage a virtual library of data review objects/reports or visualizations to be used for new projects. Work with project teams to implement and/or update reports, or create new reports as needed to ensure project-specific requirements are met.
  • Support GCI Leadership to ensure operational intelligence oversight, coordination, and development of clinical trial operations analytics (e.g., trial feasibility analysis, geography, site selection, smart metrics, analytical insight, and actionable recommendations).
  • Provides training to functional area personnel in the fundamentals of big data and clinical data review.
  • Supports with appropriate clinical trial and operational team leads to execute the process and implementation of the CGI group, to include a continuously improved decision-making loop.
  • Plays an active role in knowledge sharing and metric analytical capability building throughout Clinical Management, Strategic Sourcing, and Applied Innovation and Process Improvement functions.


  • Bachelors Degree
  • 8+ years of applicable health care, clinical or industry experience is required.
  • In-depth knowledge of clinical trial data management activities is preferred.
  • Analytic skills and knowledge of the drug development and regulatory process.

Term & Start

  • 12+ month contract - option to extend
  • Start 2 weeks from an offer
  • Remote -Ability to travel (up to 25%) Must be fully Vaccinated
  • Benefits included (Medical, Dental, Vision, 401k)